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dc.contributor.authorToraman, F
dc.contributor.authorALHAN, Cem
dc.contributor.authorKarabulut, H
dc.contributor.authorEvrenkaya, S
dc.contributor.authorGÖKSEL, Onur Selçuk
dc.contributor.authorTarcan, S
dc.date.accessioned2022-02-18T09:45:50Z
dc.date.available2022-02-18T09:45:50Z
dc.date.issued2004
dc.identifier.citationKarabulut H., Toraman F., Evrenkaya S., GÖKSEL O. S. , Tarcan S., ALHAN C., "Clopidogrel does not increase bleeding and allogenic blood transfusion in coronary artery surgery", EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, cilt.25, sa.3, ss.419-423, 2004
dc.identifier.issn1010-7940
dc.identifier.otherav_5ba2f46a-57c3-4fda-9db6-8bfe3811ead0
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177921
dc.identifier.urihttps://doi.org/10.1016/j.ejcts.2003.11.037
dc.description.abstractObjectives: Platelet dysfunction is one of the major reasons of postoperative bleeding following coronary artery surgery. The aim of this study was to evaluate the effects of clopidogrel; a specific and potent irreversible inhibitor of platelet aggregation; on bleeding and use of blood and blood products after coronary artery bypass surgery (CABG). Methods: Preoperative patient characteristics and perioperative and postoperative data were collected prospectively in 1628 consecutive patients undergoing isolated CABG performed by the same surgical and anesthesia team. Of these, 48 were receiving clopidogrel preoperatively. Of the 1628 patients, 1456 underwent elective and 172 (10.6%) underwent non-elective operation. Thirty-six (2.5%) of the elective patients and 12 (7%) of the non-elective patients were using clopidogrel, preoperatively. Baseline characteristics, chest tube output, and the need for reexploration or for blood and blood product transfusion of clopidogrel recipients and non-recipients were compared. The clopidogrel group had higher prothrombin time level (12.6 +/- 1.6; 11.5 +/- 1.7 s, P = 0.013), however comparable aPTT level (32.6 +/- 4.5 vs. 31.4 +/- 4.5 s), and platelet count (275 000 +/- 98 000 vs. 280 000 +/- 72 000 dl(-1)). Results: The need for reexploration or for blood and blood product transfusion, chest tube output, ICU length of stay (20.1 +/- 2.9 vs. 21.9 +/- 13.5 h; P = NS), and hospital length of stay (5.5 +/- 1.7 vs. 5.4 +/- 2.1 days; P = NS) were similar in clopidogrel recipients and non-recipients, respectively. Further analysis demonstrated no significant difference in use of homologous blood or fresh frozen plasma, amount of postoperative bleeding and reoperation rates for bleeding as well as length of intensive care unit and hospital stay between the clopidogrel and the control groups both in elective and non-elective patients. Conclusions: The results of this study suggest that preoperative use of clopidogrel is not associated with increased bleeding and need for surgical exploration as well as risk of blood and blood product transfusion after CABG. (C) 2003 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectRespiratory Care
dc.subjectGöğüs Hastalıkları ve Allerji
dc.subjectKardiyoloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSurgery
dc.subjectCardiology and Cardiovascular Medicine
dc.subjectPulmonary and Respiratory Medicine
dc.subjectHealth Sciences
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectSOLUNUM SİSTEMİ
dc.subjectCERRAHİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleClopidogrel does not increase bleeding and allogenic blood transfusion in coronary artery surgery
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY
dc.contributor.department, ,
dc.identifier.volume25
dc.identifier.issue3
dc.identifier.startpage419
dc.identifier.endpage423
dc.contributor.firstauthorID3372557


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